晚期黑色素瘤进展后继续使用免疫检查点抑制剂对总生存期的实际效果:来自 Melbase 队列的估计。

IF 1.5 4区 医学 Q3 DERMATOLOGY
Camille Macaire, Wendy Lefevre, Sophie Dalac, Henri Montaudié, Delphine Legoupil, Olivier Dereure, Caroline Dutriaux, Marie Thérèse Leccia, François Aubin, Jean Jacques Grob, Philippe Saiag, Julie De Quatrebarbes, Eve Maubec, Thierry Lesimple, Florence Granel-Brocard, Laurent Mortier, Stéphane Dalle, Céleste Lebbé, Chloé Prod'homme
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引用次数: 0

摘要

治疗转移性黑色素瘤的免疫检查点抑制剂(ICI)与不同类型的反应有关,因此很难评估患者的获益。一些临床试验表明,即使没有客观的放射学反应,ICI 也能为患者带来生存优势。本研究的目的是在一组终末线转移性黑色素瘤患者中评估疾病进展后继续接受 ICI 对总生存期(OS)的影响。研究人员通过法国多中心生物库 Melbase 收集了 120 名转移性黑色素瘤患者的临床数据,该生物库对不可切除的黑色素瘤进行了前瞻性登记。分为两组:在病情进展时继续接受终线 ICI 治疗的患者(治疗组)和在病情进展时停止 ICI 治疗的患者(对照组)。主要终点是进展后的OS。采用倾向得分加权法纠正适应症偏倚。在 120 名患者中,72 人(60%)继续接受 ICI 治疗。治疗组的中位生存期为4.2个月[95% 置信区间(CI)2.6-6.27],对照组的中位生存期为1.3个月(95% CI 0.95-1.74)(P < 0.0001)。计算得出的危险比为0.20(0.13-0.33)。研究发现,继续使用 ICI 与生命末期住院率较高、生命最后 15 天接受的治疗较多、使用专科姑息治疗较少有关。这项研究发现,转移性黑色素瘤患者在病情进展后继续接受终末线 ICI 治疗,其瞬时死亡概率会显著降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-life effectiveness on overall survival of continued immune checkpoint inhibition following progression in advanced melanoma: estimation from the Melbase cohort.

The link between palliative care and oncology must continue to develop, taking into account advances in treatment.Immune checkpoint inhibition (ICI) for metastatic melanoma is associated with different types of response, making it difficult to assess the benefits to the patient. Some clinical trials suggest a survival advantage of ICI even in the absence of an objective radiographic response. The aim of this study is to assess the impact of continuing ICI after progression of the disease on the overall survival (OS) in a cohort of final-line metastatic melanoma patients. Clinical data from 120 patients with metastatic melanoma were collected via Melbase, a French multicentric biobank, prospectively enrolling unresectable melanoma. Two groups were defined: patients continuing final-line ICI at progression (treated) and patients stopping ICI at progression (controls). The primary end-point is the OS from progression. Propensity score weighting was used to correct for indication bias. From the 120 patients, 72 (60%) continued ICI. Median OS from progression was 4.2 months [95% confidence interval (CI) 2.6-6.27] in the treated group and median OS was 1.3 months (95% CI 0.95-1.74) in the control group (P < 0.0001). The calculated hazard ratio was 0.20 (0.13-0.33). Continued ICI was discovered to have an association with a higher rate of hospitalization at the end of life; more treatments received in the last 15 days of life and less utilization of specialist palliative care. This study discovered that patients with metastatic melanoma show a significant decrease in the instantaneous probability of mortality when they continue with finale-line ICI after progression.

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来源期刊
Melanoma Research
Melanoma Research 医学-皮肤病学
CiteScore
3.40
自引率
4.50%
发文量
139
审稿时长
6-12 weeks
期刊介绍: ​​​​​​Melanoma Research is a well established international forum for the dissemination of new findings relating to melanoma. The aim of the Journal is to promote the level of informational exchange between those engaged in the field. Melanoma Research aims to encourage an informed and balanced view of experimental and clinical research and extend and stimulate communication and exchange of knowledge between investigators with differing areas of expertise. This will foster the development of translational research. The reporting of new clinical results and the effect and toxicity of new therapeutic agents and immunotherapy will be given emphasis by rapid publication of Short Communications. ​Thus, Melanoma Research seeks to present a coherent and up-to-date account of all aspects of investigations pertinent to melanoma. Consequently the scope of the Journal is broad, embracing the entire range of studies from fundamental and applied research in such subject areas as genetics, molecular biology, biochemistry, cell biology, photobiology, pathology, immunology, and advances in clinical oncology influencing the prevention, diagnosis and treatment of melanoma.
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